Support the Cure

Your gift is not charity. It is acceleration.

Every dollar lands in the pipeline that gets a Charcot-Marie-Tooth therapy to a patient: the registry, the biobank, the research models, and the path to first-in-human trials. You choose where yours goes. For 25 years, the Hereditary Neuropathy Foundation (HNF) has been building the infrastructure a cure actually needs, and none of it happened by accident. It happened because people gave.

Where your gift goes

HNF was founded in 2001 by a person living with CMT, and it has spent every year since turning gifts into the things research cannot move without: a global patient registry, a biobank of real samples, validated lab models, and clinical sites ready to run trials. We do not just write a check and hope. We build the road a treatment has to travel, and then we help carry the science down it.

Below you can see the numbers we stand behind, the programs your gift can power, and an honest account of where a cure stands today. Pick the path that fits you, and your money goes to work.

A smiling young girl in a rainbow dress sits on her power wheelchair in a sunny park.

By the numbers

25 years building the cure since 2001
2013 GRIN patient registry launched
100+ CMT subtypes the work reaches
$10 million CMT Cure Accelerator goal

Explore ways to give

Put your gift to work

One gift, straight into the science. The CMT Cure Accelerator moves capital to the research most likely to reach patients, and your donation is what gives it speed. Give once, give monthly, or pick the way that fits you.

Double your gift

See if your employer will match your gift

Thousands of employers match the gifts their staff give, often dollar for dollar. Search your company to see whether your gift to HNF can be doubled, with the forms and steps to make it happen.